Ahuja Vineet, Dieckgraefe Brian K, Anant Shrikant
Department of Gastroenterology, All India Institute of Medical Sciences, New Delhi, India.
Curr Opin Gastroenterol. 2006 Mar;22(2):90-4. doi: 10.1097/01.mog.0000203865.25384.65.
A concise report of published research is presented here that has provided new insights into the molecular and cell biology of the small intestine.
The precise control of cell renewal lineage commitment, differentiation and apoptosis along the crypt-villus axis are regulated by paracrine and autocrine signaling pathways that include Wnt, Hedgehog and Notch ligands. The downstream signaling pathways and transcriptional control of gene expression are being elucidated. Conditional loss of functional c-myc in the intestinal mucosa may have no effect on the normal homeostasis of this tissue. Manipulation of CUGBP2 expression may modulate the response of normal intestine to radiation therapy.
The cellular interactions at various levels in the small intestine are being understood and would provide a framework for interventional translational research in coming years.
本文简要报告已发表的研究,这些研究为小肠的分子和细胞生物学提供了新见解。
沿隐窝 - 绒毛轴的细胞更新、谱系定向、分化和凋亡的精确控制由旁分泌和自分泌信号通路调节,这些通路包括Wnt、Hedgehog和Notch配体。基因表达的下游信号通路和转录控制正在被阐明。肠道黏膜中功能性c-myc的条件性缺失可能对该组织的正常稳态没有影响。操纵CUGBP2表达可能会调节正常肠道对放射治疗的反应。
小肠中不同水平的细胞相互作用正在被理解,这将为未来几年的介入性转化研究提供框架。